Anti-IDH1 antibody [RcMab-1] - BSA and Azide free
- BOND RX™ Validated
- Recombinant
- KO Validated
- What is this?
5
(1 Review)
|
(2 Publications)
Rat Recombinant Monoclonal IDH1 antibody. Carrier free. Suitable for WB, ICC/IF, IHC-P and reacts with Rat, Human samples. Cited in 2 publications.
View Alternative Names
PICD, IDH1, Isocitrate dehydrogenase [NADP] cytoplasmic, IDH, Cytosolic NADP-isocitrate dehydrogenase, IDPc, NADP(+)-specific ICDH, Oxalosuccinate decarboxylase
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IDH1 antibody [RcMab-1] - BSA and Azide free (AB256562)
Immunohistochemical analysis of paraffin-embedded human prostatic hyperplasia tissue labeling IDH1 with ab256557 at 1/500 dilution (14.79μg/ml) followed by ready to use Goat Anti-rat IgG H&L (HRP polymer) (ab214882). Positive staining on human prostatic hyperplasia. The section was incubated with ab256557 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is ready to use Goat Anti-rat IgG H&L (HRP polymer) (ab214882).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab256557).
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-IDH1 antibody [RcMab-1] - BSA and Azide free (AB256562)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized wild-type HAP1 cells labelling IDH1 with ab256557 at 1/20 dilution (73.95μg/ml), followed by ab150157 Goat Anti-rat IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution (Green).
Confocal image showing positive staining in wild-type HAP1 cells, while no staining in IDH1 knockout HAP1 cells.
ab179513 Anti-beta Tubulin rabbit monoclonal antibody was used to counterstain tubulin at 1/200 dilution, followed by ab150080 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) at a 1/1000 dilution (Red). The nuclear counterstain was DAPI (Blue).
Secondary antibody only controls.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab256557).
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IDH1 antibody [RcMab-1] - BSA and Azide free (AB256562)
Immunohistochemical analysis of paraffin-embedded human normal cerebrum tissue labeling IDH1 with ab256557 at 1/500 dilution (14.79μg/ml) followed by ready to use Goat Anti-rat IgG H&L (HRP polymer) (ab214882). The section was incubated with ab256557 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Negative control : No staining on human normal cerebrum.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab256557).
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IDH1 antibody [RcMab-1] - BSA and Azide free (AB256562)
Immunohistochemical analysis of paraffin-embedded human kidney tissue labeling IDH1 with ab256557 at 1/500 dilution (14.79μg/ml) followed by ready to use Goat Anti-rat IgG H&L (HRP polymer) (ab214882). Positive staining on human kidney tissue. The section was incubated with ab256557 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is ready to use Goat Anti-rat IgG H&L (HRP polymer) (ab214882).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab256557).
- WB
Lab
Western blot - Anti-IDH1 antibody [RcMab-1] - BSA and Azide free (AB256562)
Blocking/Dilution buffer : 5% NFDM/TBST.
Exposure times : Lane 1 : 3 minutes; Lanes 2-3 : 3 seconds.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab256557).
All lanes:
Western blot - Anti-IDH1 antibody [RcMab-1] (<a href='/en-us/products/primary-antibodies/idh1-antibody-rcmab-1-ab256557'>ab256557</a>) at 1.479 µg/mL
Lane 1:
PC-12 (rat adrenal gland pheochromocytoma), whole cell lysate at 10 µg
Lane 2:
Rat heart tissue lysate at 10 µg
Lane 3:
Human heart tissue lysate at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rat IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rat-igg-h-l-hrp-ab205720'>ab205720</a>) at 1/10000 dilution
Predicted band size: 46 kDa
false
- WB
Lab
Western blot - Anti-IDH1 antibody [RcMab-1] - BSA and Azide free (AB256562)
Blocking/Dilution buffer : 5% NFDM/TBST.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab256557).
All lanes:
Western blot - Anti-IDH1 antibody [RcMab-1] (<a href='/en-us/products/primary-antibodies/idh1-antibody-rcmab-1-ab256557'>ab256557</a>) at 1.479 µg/mL
Lane 1:
Wild type HAP1 whole cell lysate at 20 µg
Lane 2:
IDH1 knockout HAP1 whole cell lysate at 20 µg
Lane 3:
HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate at 20 µg
Lane 4:
HepG2 (human hepatocellular carcinoma epithelial cell), whole cell lysate at 20 µg
Lane 5:
Raji (human Burkitt's lymphoma B lymphocyte), whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rat IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rat-igg-h-l-hrp-ab205720'>ab205720</a>) at 1/10000 dilution
Predicted band size: 46 kDa
false
Exposure time: 8s
Related conjugates and formulations (1)
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Anti-IDH1 antibody [RcMab-1]
Reactivity data
Product details
ab256562 is the carrier-free version of ab256557.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Want a custom formulation?
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Isocitrate dehydrogenase 1 plays an important role in cellular metabolism by helping to maintain the NADP+/NADPH balance important for redox reactions. This enzyme operates mainly as a homodimer meaning two identical subunits form a complex for functional activity. It contributes significantly to lipid and glucose metabolism due to its production of NADPH which the cells use for biosynthetic pathways and detoxification.
Pathways
The involvement of IDH1 in the citric acid cycle highlights its importance in energy production and metabolic regulation. This enzyme closely associates with other metabolic enzymes such as IDH2 another member of the isocitrate dehydrogenase family found in mitochondria suggesting a coordinated function between cytoplasmic and mitochondrial metabolism. Beyond its role in the citric acid cycle IDH1 also relates to the pentose phosphate pathway an alternative glucose metabolism route providing reducing equivalents and ribose 5-phosphate for nucleotide synthesis.
Product protocols
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Target data
Publications (2)
Recent publications for all applications. Explore the full list and refine your search
Oncogene 44:2689-2714 PubMed40394416
2025
Applications
Unspecified application
Species
Unspecified reactive species
The Tohoku journal of experimental medicine 230:103-9 PubMed23782684
2013
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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